在成人发病的肌张力障碍中传播的风险。

IF 2.5 Q2 CLINICAL NEUROLOGY
Tremor and Other Hyperkinetic Movements Pub Date : 2024-12-04 eCollection Date: 2024-01-01 DOI:10.5334/tohm.952
Esra Kochan Kizilkilic, Nursena Erener, Mustafa Meric, Nurten Uzun Adatepe, Aysegul Gunduz
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引用次数: 0

摘要

背景:成人发病的肌张力障碍也可以扩散到身体的其他部位,尽管它不像儿童发病的肌张力障碍那么常见。目的:我们的研究旨在探讨在所有成人发病的肌张力障碍类型中决定其扩散模式的临床因素。方法:我们回顾性分析了在本中心诊断为孤立性肌张力障碍的患者的病历。我们纳入了18年后报告出现症状的患者。然后比较有无扩散组的临床因素。结果:434例患者(局灶性肌张力障碍396例,节段性肌张力障碍29例,全身性肌张力障碍9例)。平均随访8.6±7.8年),48例(11.1%)出现肌张力障碍扩散,其中37例为局灶性肌张力障碍向节段性肌张力障碍发展,2例为局灶性肌张力障碍向全身性肌张力障碍发展,2例为节段性肌张力障碍向全身性肌张力障碍发展,7例为局灶性肌张力障碍向节段性肌张力障碍发展。眼睑痉挛是最常见的局灶性肌张力障碍,其次是口下颌肌张力障碍、颈肌张力障碍、喉肌张力障碍和上肢肌张力障碍。在大约十分之一的肌张力障碍患者中观察到扩散模式,并且在节段性肌张力障碍组中扩散更为频繁。虽然扩散组在感觉障碍、震颤和性别方面没有差异,但家族史在非扩散组中更为常见(p = 0.023)。发病年龄越大与扩散几率增加独立相关(危险比:1.054,p < 0.001, B = 0.053)。结论:虽然扩散的危险因素是可变的,但潜在的机制尚不完全清楚。遗传因素可能与该病的传播有关,有待进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Risk of Spreading in Adult-onset Dystonia.

Background: Adult-onset dystonia can also spread to other parts of the body, although it is not as common as childhood-onset dystonia.

Objective: Our study aimed to examine the clinical factors determining spreading patterns in all adult-onset dystonia types.

Methods: We retrospectively analyzed the medical records of patients with a diagnosis of isolated dystonia followed longitudinally at our center. We included patients reporting symptom onset after 18 years. We then compared the clinical factors between groups with and without spreading.

Results: Among 434 patients (396 focal, 29 segmental, and nine generalized onset dystonia. mean follow-up of 8.6 ± 7.8 years), 48 (11.1%) experienced spread of dystonia, with 37 progressing from focal to segmental, two from focal to generalized, two from segmental to generalized, and seven from focal to segmental to generalized dystonia. Blepharospasm was the most common focal dystonia noted to spread, followed by oromandibular dystonia, cervical dystonia, laryngeal dystonia, and upper extremity dystonia, in decreasing order. A spreading pattern was observed in approximately one in 10 dystonia patients, and the spreading was more frequent in the segmental dystonia group. While there was no difference between the spreading groups regarding sensory tricks, tremor, and gender, family history was more common in the non-spreading group (p = 0.023). Older age at onset was independently associated with increased odds of spreading (hazards ratio: 1.054, p < 0.001, B = 0.053).

Conclusion: Although risk factors for spread are variable, the underlying mechanisms are not fully known. Genetic factors may be possibly related to the spread, and future studies are needed on this subject.

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来源期刊
CiteScore
4.00
自引率
4.50%
发文量
31
审稿时长
6 weeks
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